AI Article Synopsis

  • Metabolic syndrome (MS) is a significant public health issue globally, characterized by obesity, hypertension, dyslipidaemia, and insulin resistance, and its relationship with cancer risk is not fully understood.
  • The study aims to compare the risk of 14 types of cancer associated with MS against the risks posed by individual components of MS and will track cancer onset after MS diagnosis between 2006-2017, focusing on sex differences.
  • A case-control and cohort study will utilize data from the SIDIAP database, involving demographic matching and analyses to evaluate associations and time intervals, with ethical approval obtained and results planned for publication and presentation.

Article Abstract

Background: Metabolic syndrome (MS) is defined by the clustering of specific metabolic disorders in one subject. MS is highly prevalent globally and currently considered a growing public health concern. MS comprises obesity, hypertension, dyslipidaemia and insulin resistance. Mechanisms linking MS with cancer are poorly understood, and it is as yet unknown if MS confers a greater risk than the risk entailed by each of its separate components. The main objective of this study is to compare the association between MS and 14 site-specific cancer against the association between one or two individual components of MS and cancer. The secondary objective is to evaluate the time elapsed since the diagnosis of MS and the subsequent onset of cancer within the 2006-2017 period by sex.

Methods And Analysis: A case-control study will be conducted for the main objective and a cohort of patients with MS will be followed for the evaluation of the second objective. Incident cases of fourteen types of cancer in patients ≥40 years of age diagnosed prospectively will be selected from electronic primary care records in the Information System for Research in Primary Care (SIDIAP database; www.sidiap.org). The SIDIAP database includes anonymous data from 6 million people (80% of the Catalan population) registered in 286 primary healthcare centres. Each matched control (four controls for each case) will have the same inclusion date, the same sex and age (±1 year) than the paired case. Logistic regression and a descriptive analysis and Kaplan-Meier analysis will be performed, in accordance with the objectives.

Ethics And Dissemination: The protocol of the study was approved by the IDIAP Jordi Gol Clinical Research Ethics Committee (protocol P17/212). The study's findings will be published in a peer-reviewed journal and disseminated at national and international conferences and oral presentations to researchers, clinicians and policy makers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6575640PMC
http://dx.doi.org/10.1136/bmjopen-2018-025365DOI Listing

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